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TACO1 Gene Leigh syndrome due to the mitochondrial complex IV deficiency Genetic Test

4,400 د.إ

-21%

The TACO1 gene Leigh syndrome due to the mitochondrial complex IV deficiency genetic test is a specialized diagnostic tool designed to identify mutations in the TACO1 gene, which are associated with Leigh syndrome, a severe neurological disorder. This condition is characterized by mitochondrial complex IV deficiency, leading to a range of symptoms such as psychomotor regression, hypotonia, and respiratory abnormalities. The test is crucial for early diagnosis and management of the syndrome, providing essential information for personalized treatment plans.

Conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing capabilities, the test offers a comprehensive analysis of the TACO1 gene to detect any mutations that could be responsible for the condition. With a cost of 4400 AED, it represents a significant investment in the health and well-being of individuals at risk of or suspected to have Leigh syndrome. Early detection through this genetic test can be pivotal in managing the syndrome’s progression and improving the quality of life for affected individuals.

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TACO1 Gene Leigh Syndrome Genetic Test

At DNA Labs UAE, we offer the TACO1 Gene Leigh Syndrome Genetic Test to diagnose mitochondrial complex IV deficiency, which is associated with Leigh syndrome. This severe neurological disorder typically manifests in infancy or early childhood and is characterized by progressive loss of motor and cognitive abilities, muscle weakness, respiratory problems, and other symptoms.

Test Details

The TACO1 gene is closely linked to Leigh syndrome and mitochondrial complex IV deficiency. Our NGS (Next-Generation Sequencing) genetic testing method allows for the simultaneous analysis of multiple genes or the entire genome. By identifying mutations in the TACO1 gene or other genes associated with mitochondrial complex IV deficiency, our test can provide a definitive diagnosis and guide treatment options.

Test Components and Price

The TACO1 Gene Leigh Syndrome Genetic Test is priced at AED 4400.0. We accept blood samples, extracted DNA, or one drop of blood on an FTA Card as sample conditions.

Report Delivery and Turnaround Time

Once the sample is received, the report will be delivered within 3 to 4 weeks. Our team of experts will thoroughly analyze the genetic data to provide accurate and reliable results.

Referring Doctor and Test Department

This test is recommended by neurologists and falls under the Genetics department at DNA Labs UAE.

Pre Test Information

Prior to the test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by TACO1 Gene Leigh Syndrome due to mitochondrial complex IV deficiency.

Benefits of TACO1 Gene Leigh Syndrome Genetic Test

By identifying the specific genetic mutations causing Leigh syndrome, this test can not only provide a definitive diagnosis but also help in planning treatment and management options. It can also provide information about the likelihood of the condition being passed on to future generations.

Test Name TACO1 Gene Leigh syndrome due to the mitochondrial complex IV deficiency Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for TACO1 Gene Leigh syndrome due to the mitochondrial complex IV deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with TACO1 Gene Leigh syndrome due to the mitochondrial complex IV deficiency
Test Details

The TACO1 gene is associated with Leigh syndrome, a severe neurological disorder that typically presents in infancy or early childhood. Leigh syndrome is characterized by progressive loss of motor and cognitive abilities, muscle weakness, respiratory problems, and other symptoms.

Mitochondrial complex IV deficiency, also known as cytochrome c oxidase deficiency, is a type of mitochondrial disease that affects the function of complex IV in the electron transport chain. This deficiency impairs the ability of cells to produce energy, leading to the symptoms associated with Leigh syndrome.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or the entire genome. In the case of Leigh syndrome, NGS genetic testing can be used to identify mutations in the TACO1 gene or other genes associated with mitochondrial complex IV deficiency.

By identifying the specific genetic mutations causing Leigh syndrome, NGS genetic testing can provide a definitive diagnosis and help guide treatment and management options. It can also provide information about the likelihood of the condition being passed on to future generations.